A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691261



Internal ID15081227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50827676..50829414hg38UCSC Ensembl
Innerchr19:51330932..51332670hg19UCSC Ensembl
Innerchr19:56022744..56024482hg18UCSC Ensembl
Innerchr19:56022744..56024482hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg381739
hg191739
hg181739
hg171739
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515608
Supporting Variants
Samples
Known GenesKLK15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691261
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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